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- W2058596524 abstract "Von Hippel-Lindau (VHL) disease is an autosomal dominant disorder that results from a germline mutation of the VHL gene. The affected individuals might develop several benign or malignant tumors such as central nervous system or retinal haemangioblastomas, endolymphatic sac tumors, renal cell carcinomas, pheochromocytomas or pancreatic cysts and neuroendocrine tumors. We report here on a case of a 21 year old female with von Hippel-Lindau disease and she presented with only pancreatic neuroendocrine tumor and no evidence of haemangioblastomas or other visceral complications. Further, direct sequencing of the VHL gene reveals a novel germline frameshift mutation of codon 198 from the deletion of nucleotide 592 (cytosine), leading to truncation of the VHL protein." @default.
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- W2058596524 date "2011-01-01" @default.
- W2058596524 modified "2023-10-14" @default.
- W2058596524 title "A Case of von Hippel-Lindau Disease Presenting with Pancreatic Neuroendocrine Tumor" @default.
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- W2058596524 doi "https://doi.org/10.3803/enm.2011.26.1.89" @default.
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